Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1559414131 | 1.000 | 0.080 | 3 | 38709556 | inframe deletion | AGA/- | delins | 1 | |||
rs57326399 | 1.000 | 0.080 | 3 | 38726809 | missense variant | T/C | snv | 0.24 | 0.21 | 1 | |
rs6599240 | 1.000 | 0.080 | 3 | 38697226 | 3 prime UTR variant | G/A | snv | 0.44 | 1 | ||
rs6599257 | 1.000 | 0.080 | 3 | 38763097 | intron variant | C/T | snv | 0.74 | 1 | ||
rs7428167 | 1.000 | 0.080 | 3 | 38736700 | intron variant | T/C | snv | 0.59 | 1 | ||
rs7430439 | 1.000 | 0.080 | 3 | 38762148 | intron variant | G/A | snv | 0.66 | 1 | ||
rs7641844 | 1.000 | 0.080 | 3 | 38760760 | intron variant | A/G | snv | 0.33 | 0.31 | 1 | |
rs774893568 | 1.000 | 0.080 | 3 | 38714013 | missense variant | C/T | snv | 4.4E-05 | 7.0E-05 | 1 | |
rs9874633 | 1.000 | 0.080 | 3 | 38730503 | intron variant | A/G | snv | 0.38 | 1 | ||
rs267607028 | 0.925 | 0.080 | 19 | 35033827 | stop gained | G/A | snv | 8.0E-06 | 2 | ||
rs267607029 | 0.925 | 0.080 | 19 | 35033828 | stop gained | G/A | snv | 2 | |||
rs587777023 | 1.000 | 0.080 | 11 | 118166903 | missense variant | T/C | snv | 8.0E-06 | 2.1E-05 | 1 | |
rs147205617 | 1.000 | 0.080 | 11 | 123642563 | missense variant | C/T | snv | 3.1E-04 | 3.1E-04 | 2 | |
rs121918282 | 0.882 | 0.080 | 11 | 123653773 | missense variant | A/G | snv | 2.0E-04 | 3.5E-04 | 3 | |
rs1064794243 | 0.851 | 0.200 | 17 | 63941169 | missense variant | A/T | snv | 5 | |||
rs1805124 | 0.742 | 0.280 | 3 | 38603929 | missense variant | T/C | snv | 0.22 | 0.25 | 16 | |
rs137854618 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 15 | ||
rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 15 | ||
rs41261344 | 0.763 | 0.120 | 3 | 38575385 | missense variant | C/T | snv | 5.4E-03 | 2.2E-03 | 11 | |
rs137854601 | 0.776 | 0.120 | 3 | 38551022 | stop gained | C/A;T | snv | 4.0E-06 | 10 | ||
rs199473097 | 0.763 | 0.120 | 3 | 38606710 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 9 | |
rs757532106 | 0.763 | 0.120 | 3 | 38550500 | stop gained | G/A | snv | 4.5E-05 | 4.9E-05 | 9 | |
rs199473605 | 0.851 | 0.120 | 3 | 38560374 | missense variant | C/G;T | snv | 4.8E-05; 4.0E-06 | 7 | ||
rs11708996 | 0.925 | 0.120 | 3 | 38592432 | intron variant | G/C | snv | 0.11 | 6 | ||
rs137854600 | 0.807 | 0.120 | 3 | 38551504 | missense variant | C/A;T | snv | 6 |